ENST00000461280.2:n.1010T>G
|
|
|
ENST00000684241.1:n.2545T>G
|
|
|
ENST00000262186.10:c.1712T>G
MANE Select
|
ENSP00000262186.5:p.Ile571Ser
|
|
ENST00000330883.9:c.692T>G
|
ENSP00000328531.4:p.Ile231Ser
|
|
ENST00000262186.9:c.1712T>G
|
ENSP00000262186.5:p.Ile571Ser
|
|
ENST00000330883.8:c.692T>G
|
ENSP00000328531.4:p.Ile231Ser
|
|
ENST00000430723.4:c.1364T>G
|
ENSP00000387657.4:p.Ile455Ser
|
|
ENST00000461280.1:n.999T>G
|
|
|
ENST00000473610.5:n.1017T>G
|
|
|
ENST00000532957.5:n.1935T>G
|
|
|
NM_000238.3:c.1712T>G , LRG_288t1:c.1712T>G
|
NP_000229.1:p.Ile571Ser
|
|
NM_001204798.1:c.692T>G
|
NP_001191727.1:p.Ile231Ser
|
|
NM_172056.2:c.1712T>G , LRG_288t2:c.1712T>G
|
NP_742053.1:p.Ile571Ser
|
|
NM_172057.2:c.692T>G , LRG_288t3:c.692T>G
|
NP_742054.1:p.Ile231Ser
|
|
XM_011516185.1:c.1412T>G
|
XP_011514487.1:p.Ile471Ser
|
|
XM_011516186.1:c.1712T>G
|
XP_011514488.1:p.Ile571Ser
|
|
XM_011516185.2:c.1412T>G
|
XP_011514487.1:p.Ile471Ser
|
|
XM_011516186.3:c.1712T>G
|
XP_011514488.1:p.Ile571Ser
|
|
XM_017012195.1:c.1562T>G
|
XP_016867684.1:p.Ile521Ser
|
|
XM_017012196.1:c.1535T>G
|
XP_016867685.1:p.Ile512Ser
|
|
NM_000238.4:c.1712T>G
MANE Select
|
NP_000229.1:p.Ile571Ser
|
|
NM_001204798.2:c.692T>G
|
NP_001191727.1:p.Ile231Ser
|
|
NM_172057.3:c.692T>G
|
NP_742054.1:p.Ile231Ser
|
|